Canonical Allele Identifier: CA1946816779

Gene: CYP2E1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133538833T= , CM000672.2:g.133538833T=	GRCh38
NC_000010.10:g.135352337T= , CM000672.1:g.135352337T=	GRCh37
NC_000010.9:g.135202327T=	NCBI36
NG_008383.1:g.16471T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252945.8:c.1351T= MANE Select	ENSP00000252945.3:p.Leu451=
ENST00000252945.7:c.1351T=	ENSP00000252945.3:p.Leu451=
ENST00000368520.1:n.1358+941T=
ENST00000463117.6:c.1351T=	ENSP00000440689.1:p.Leu451=
ENST00000469258.1:n.447T=
NM_000773.3:c.1351T=	NP_000764.1:p.Leu451=
NM_000773.4:c.1351T= MANE Select	NP_000764.1:p.Leu451=